Coils
Target XL
A non-bioabsorbable, implantable device intended to induce a neurovascular thrombosis to treat an intracranial aneurysm and/or neurovascular arteriovenous malformation (AVM); it may also be intended to treat non-neurovascular malformations. It is in the form of a metal [e.g., platinum alloy] or metal/synthetic polymer wire which coils upon deployment within the aneurysm/vasculature; it is typically pre-attached to a nonimplantable delivery wire. Disposable devices associated with implantation (e.g., delivery wire, catheter) may be included.
Target XL models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| M0036101040 | — | MR Conditional | Available |
| M0036101240 | — | MR Conditional | Available |
| M0036101450 | — | MR Conditional | Available |
| M0036101650 | — | MR Conditional | Available |
| M0036101850 | — | MR Conditional | Available |
| M0036102050 | — | MR Conditional | Available |
| M0036102250 | — | MR Conditional | Available |
| M0036102450 | — | MR Conditional | Available |
| M0036106200 | — | MR Conditional | Available |
| M0036107200 | — | MR Conditional | Available |
| M0036108300 | — | MR Conditional | Available |
| M0036109300 | — | MR Conditional | Available |
| M0036111040 | — | MR Conditional | Available |
| M0036111250 | — | MR Conditional | Available |
| M0036111450 | — | MR Conditional | Available |
| M0036111650 | — | MR Conditional | Available |
| M0036111850 | — | MR Conditional | Available |
| M0036112050 | — | MR Conditional | Available |
| M0036112250 | — | MR Conditional | Available |
| M0036112450 | — | MR Conditional | Available |
| M0036115150 | — | MR Conditional | Available |
| M0036116200 | — | MR Conditional | Available |
| M0036117200 | — | MR Conditional | Available |
| M0036118300 | — | MR Conditional | Available |
| M0036119300 | — | MR Conditional | Available |
| M0036121040 | — | MR Conditional | Available |
| M0036121240 | — | MR Conditional | Available |
| M0036121450 | — | MR Conditional | Available |
| M0036121650 | — | MR Conditional | Available |
| M0036121850 | — | MR Conditional | Available |
| M0036122030 | — | MR Conditional | Available |
| M0036122050 | — | MR Conditional | Available |
| M0036122060 | — | MR Conditional | Available |
| M0036123060 | — | MR Conditional | Available |
| M0036123090 | — | MR Conditional | Available |
| M0036124080 | — | MR Conditional | Available |
| M0036124120 | — | MR Conditional | Available |
| M0036125100 | — | MR Conditional | Available |
| M0036125150 | — | MR Conditional | Available |
| M0036126200 | — | MR Conditional | Available |
| M0036127200 | — | MR Conditional | Available |
| M0036128300 | — | MR Conditional | Available |
| M0036129300 | — | MR Conditional | Available |
Procedures that use coils
Frequently asked questions
What is Target XL used for?
A non-bioabsorbable, implantable device intended to induce a neurovascular thrombosis to treat an intracranial aneurysm and/or neurovascular arteriovenous malformation (AVM); it may also be intended to treat non-neurovascular malformations. It is in the form of a metal [e.g., platinum alloy] or metal/synthetic polymer wire which coils upon deployment within the aneurysm/vasculature; it is typically pre-attached to a nonimplantable delivery wire. Disposable devices associated with implantation (e.g., delivery wire, catheter) may be included.
Who makes Target XL?
Target XL is made by Stryker Corporation. It is listed under embolization coils in our device library.
What sizes does Target XL come in?
The FDA device database does not list sizes for Target XL. Check the instructions for use or ask a Stryker Corporation representative.
Is Target XL MRI safe?
The FDA device database lists Target XL as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Target XL FDA cleared?
Target XL is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Stryker Corporation sales representative?
Stryker Corporation has not listed representatives on LA Vascular yet. Visit the Stryker Corporation company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.